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481 results

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Next-generation-sequencing-based risk stratification and identification of new genes involved in structural and sequence variations in near haploid lymphoblastic leukemia.
Chen C, Bartenhagen C, Gombert M, Okpanyi V, Binder V, Röttgers S, Bradtke J, Teigler-Schlegel A, Harbott J, Ginzel S, Thiele R, Fischer U, Dugas M, Hu J, Borkhardt A. Chen C, et al. Among authors: borkhardt a. Genes Chromosomes Cancer. 2013 Jun;52(6):564-79. doi: 10.1002/gcc.22054. Epub 2013 Mar 18. Genes Chromosomes Cancer. 2013. PMID: 23508829
Whole-genome paired-end analysis confirms remarkable genomic stability of atypical teratoid/rhabdoid tumors.
Hoell JI, Gombert M, Bartenhagen C, Ginzel S, Husemann P, Felsberg J, Reifenberger G, Eggert A, Dugas M, Schönberger S, Borkhardt A, Fischer U. Hoell JI, et al. Among authors: borkhardt a. Genes Chromosomes Cancer. 2013 Oct;52(10):983-5. doi: 10.1002/gcc.22092. Epub 2013 Aug 9. Genes Chromosomes Cancer. 2013. PMID: 23929726 No abstract available.
RAG1 deficiency with a shifting B cell phenotype and chromosomal instability.
Ghosh S, Hönscheid A, Schwarz K, Eirich K, Schindler D, Schönberger S, Speckmann C, Borkhardt A, Laws HJ. Ghosh S, et al. Among authors: borkhardt a. Clin Immunol. 2014 May-Jun;152(1-2):65-7. doi: 10.1016/j.clim.2014.02.009. Epub 2014 Feb 26. Clin Immunol. 2014. PMID: 24583411 No abstract available.
Recurrent RHOA mutations in pediatric Burkitt lymphoma treated according to the NHL-BFM protocols.
Rohde M, Richter J, Schlesner M, Betts MJ, Claviez A, Bonn BR, Zimmermann M, Damm-Welk C, Russell RB, Borkhardt A, Eils R, Hoell JI, Szczepanowski M, Oschlies I, Klapper W, Burkhardt B, Siebert R; German ICGC MMML-Seq-Project; NHL-BFM Study Group. Rohde M, et al. Among authors: borkhardt a. Genes Chromosomes Cancer. 2014 Nov;53(11):911-6. doi: 10.1002/gcc.22202. Epub 2014 Jul 8. Genes Chromosomes Cancer. 2014. PMID: 25044415
A new workflow for whole-genome sequencing of single human cells.
Binder V, Bartenhagen C, Okpanyi V, Gombert M, Moehlendick B, Behrens B, Klein HU, Rieder H, Ida Krell PF, Dugas M, Stoecklein NH, Borkhardt A. Binder V, et al. Among authors: borkhardt a. Hum Mutat. 2014 Oct;35(10):1260-70. doi: 10.1002/humu.22625. Epub 2014 Aug 18. Hum Mutat. 2014. PMID: 25066732
Next-generation-sequencing of recurrent childhood high hyperdiploid acute lymphoblastic leukemia reveals mutations typically associated with high risk patients.
Chen C, Bartenhagen C, Gombert M, Okpanyi V, Binder V, Röttgers S, Bradtke J, Teigler-Schlegel A, Harbott J, Ginzel S, Thiele R, Husemann P, Krell PF, Borkhardt A, Dugas M, Hu J, Fischer U. Chen C, et al. Among authors: borkhardt a. Leuk Res. 2015 Sep;39(9):990-1001. doi: 10.1016/j.leukres.2015.06.005. Epub 2015 Jun 14. Leuk Res. 2015. PMID: 26189108
481 results